Digital Health Project Nurse

2 weeks ago

Coventry, Coventry, United Kingdom University Hospitals Coventry and Warwickshire Full time

Work autonomously to manage a caseload of patients acting as a professional to ensure care to patients is delivered according to Trust policies and procedures and the research protocol delivery high standards and continuity of clinical care for study participants.


  • Attend Multi-disciplinary Meetings, and appropriate clinics, to assess volunteers/patients for eligibility for research and recruit new patients, to act as a resource to the members of the MDT.
  • Ensure that trial specific clinical investigations / procedures are undertaken as required by the research protocol in order to establish eligibility and maintain safety in the trial by all team members.
  • Ensure safe and appropriate storage of specimens in accordance with trial protocols and regulatory / Trust guidance.
  • Ensure all team members undertake relevant training and assessment of competence, working within scope of professional practice prior to undertaking any clinical procedures / administration of treatments associated with the research treatment regimes.
  • Ensure the safe administration of treatments and drugs that are given within the context of a clinical trial by all team members.
  • Ensure all staff record and report adverse /serious adverse events as classified in the study protocol criteria which occur whilst patient is in the clinical trial e.g. hospital admission since last study visit
  • Ensure accurate documentation of patient's events in nursing/medical notes and study specific case report forms.
  • Provide ongoing information, education and support to patients (and their significant others) regarding clinical trials and their care.
Research and Portfolio Management

  • Lead in the delivery of studies within the relevant specialities ensuring they meet the requirements with regards to the Department of Health's Research Governance Framework for Health and Social Care and the EU Clinical Trials legislation by implementing quality systems.
  • Assist in the review of study protocols and contribute to the feasibility/study selection process, advising on safety, regulatory and logistical issues.
  • Liaise with RD&I Set Up Team staff contributing to the process of gaining local regulatory committee approval where required to ensure efficient service is delivered to sponsors.
  • Work with the research teams and investigators to develop strategies to overcome barriers to recruitment and solve other problems relating to specific studies.
  • Following appropriate training and competence assessment receive written informed consent from participants for allocated research studies in accordance with study protocol and Trust guidance.
  • Following appropriate training and competence assessment act as an assessor for the process of informed consent for research according to Trust guidelines.
  • Randomise / enrol patients into clinical trials or other research studies.
  • Assess and evaluate the progress of on-going clinical trials and research identifying resource implications for the teams.
  • Co-ordinate the monthly local portfolio team performance meetings: identify and act on issues.
  • Ensure accurate records for all research projects that are overseen within allocated teams are kept in accordance with all regulatory requirements including the data protection act
  • Provide advice and support to other members of the research and multidisciplinary team with regard to research governance.
  • Ensure self and team members respond to data queries generated by the study co-ordinating team within a timely manner.
  • Ensure all team members maintain accurate records of study recruitment as per local procedure and status of studies providing regular updates. This will involve ensuring that EDGE (local patient management system) is updated with key trial data and feeding back through the local portfolio team meetings

To ensure that we provide world-class patient care, UHCW recruits people that can demonstrate the Trust's Values and Behaviours in their everyday life.

You will be expected to provide us with examples from work experience and/or personal life which demonstrate these values through your behaviour.

All applicants who have a disability and who meet the minimum criteria for the job will be interviewed.

In submitting an application form, you authorise University Hospital Coventry & Warwickshire NHS Trust to confirm from your previous or current NHS employer and other prior employers; previous NHS service details and personal data held about you, including Occupational Health data (inoculations and screening tests).

This data will be transferred using NHS Electronic Staff Record and third-party systems via an automated process and only used for the purposes of obtaining and maintaining accurate employment records, should you be appointed to the post.

UHCW NHS Trust, by virtue of its Green Plan, is committed to ensuring that the way we provide services minimises the impact on the environment and the future health of the public e.g.

zero waste to landfill, reducing our carbon footprint and increasing our recycling and reuse percentages.

We will ask you to submit proof of your identity and right to work documents via a secure digital platform approved by the Home Office, named TrustID.

Alternatively, you may be asked to attend our office with original documents.
please check your account regularly including your Junk/SPAM folders

This post is subject to the Rehabilitation of Offenders Act 1974 (Exceptions) Order 1975 (Amendment) (England and Wales) Order 2020 and it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service.

Welcoming Applicants with a Disability (PDF, 53.

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